A Phase 1b/2 Study of Ibrutinib Combination Therapy in Selected Advanced Gastrointestinal and Genitourinary Tumors

Status: Completed
Location: See all (65) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The purpose of this study is to evaluate the safety, tolerability, and efficacy of single agent ibrutinib or the combination treatments of ibrutinib with everolimus, paclitaxel, docetaxel, pembrolizumab or cetuximab in selected advance gastrointestinal and genitourinary tumors.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• RCC (clear cell), urothelial carcinoma (UC) (transitional cell), gastric or gastro-esophageal junctional (GEJ) adenocarcinoma, or K-RAS or N-RAS wild-type EGFR expressing CRC For cohort 1 RCC: minimum of 1 and maximum of 4 prior regimens, one or more of which must have included a VEGF-TKI For UC cohort 2: minimum of 1 and maximum of 2 prior regimens, one of which must have included a platinum-based regimen For UC cohort 5: Minimum of 1 and maximum of 2 prior regimens, one of which must have included a checkpoint inhibitor.

• For UC cohort 6:

• Locally advanced or mUC who are not eligible for cisplatin chemo with a PDL-1 score (CPS) of ≥ 10 without prior treatment.

• Locally advanced or mUC who have progressed on platinum chemo or within 12 months of neo- or adjuvant therapy with a platinum chemotherapy. A minimum of 1 and maximum of 2 prior therapies.

• For cohort 3 gastric or GEJ adenocarcinoma: minimum of 1 and maximum of 3 prior regimens one of which must have included a fluoropyrimidine regimen For cohort 4 CRC: minimum of 2 and maximum of 4 prior regimens, which must have included both an irinotecan and an oxaliplatin based regimen unless unable to tolerate irinotecan chemotherapy

• Laboratory:

• Adequate hematologic function:

• Absolute neutrophil count ≥1500 cells/mm3 (1.5 x 109/L) Platelet count \>80,000 cells/mm3 (80 x 109/L) for cohort 1 (RCC) Platelet counts \>100,000 cells/mm3 (100 x 109/L) for all UC cohorts Hemoglobin ≥8.0 g/dL. for cohort 1 (RCC),all UC cohorts, and cohort 3 (GC) Hemoglobin ≥9.0 g/dL for cohort 4 (CRC)

• Adequate hepatic and renal function defined as:

• Serum aspartate transaminase (AST) and/or alanine transaminase (ALT) ≤5.0 x upper limit of normal (ULN) if liver metastases, or ≤3 x ULN without liver metastases Alkaline phosphatase \<3.0 x ULN or ≤5.0 x ULN if liver or bone metastases present Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin, such as hemolysis) with the exception of subjects in the GC cohort where docetaxel is administered, these subjects must have bilirubin within normal limits (WNL) Estimated Creatinine Clearance ≥30 mL/min (Cockcroft-Gault)

Locations
United States
Alabama
Clearview Cancer Institute /ID# 1128-0965
Huntsville
Arizona
Banner MD Anderson Cancer Center /ID# 1128-0802
Gilbert
University of Arizona Cancer Center - Tucson /ID# 1128-1546
Tucson
California
Alta Bates Comprehensive Cancer Center /ID# 1128-0135
Berkeley
St Marys Medical Center /ID# 1128-0969
Daly City
Duplicate_University of California San Diego/ Moores Cancer Center /ID# 1128-0241
La Jolla
VA Long Beach Healthcare System /ID# 1128-0480
Long Beach
USC Norris Cancer Center /ID# 1128-0209
Los Angeles
UC Irvine Medical Center - Chao Family Comprehensive Cancer Center /ID# 1128-0008
Orange
Gregory Smith, MD (Private Practice) /ID# 1128-0419
Saint Helena
Salinas Valley Memorial Hosp /ID# 1128-0482
Salinas
Premiere Oncology, A Medical Corporation /ID# 1128-1085
Santa Monica
St. Joseph Health /ID# 1128-1462
Santa Rosa
Connecticut
Whittingham Cancer Center at Norwalk Hospital /ID# 1128-0411
Norwalk
Washington, D.c.
Georgetown University Hospital /ID# 1128-0824
Washington
Florida
Duplicate_Cancer Specialist of North Florida (CSNF) ( R ) /ID# 1128-1093
Jacksonville
Georgia
IACT Health-Columbus /ID# 1128-1389
Columbus
Iowa
University of Iowa Hospitals and Clinics /ID# 1128-0766
Iowa City
Illinois
Northshore Kellogg Cancer Center /ID# 1128-0484
Evanston
Indiana
Franciscan Health Indianapolis /ID# 1128-1125
Indianapolis
Horizon Oncology Research Center /ID# 1128-0337
Lafayette
Kansas
The University of Kansas Cancer Center /ID# 1128-0706
Fairway
Louisiana
East Jefferson General Hospital /ID# 1128-1084
Metairie
Massachusetts
Duplicate_Tufts Medical Center /ID# 1128-0016
Boston
Michigan
Barbara Ann Karmanos Cancer In /ID# 1128-0130
Detroit
Henry Ford Hospital /ID# 1128-0195
Detroit
Missouri
Central Care Cancer Center /ID# 1128-1596
Bolivar
Capital Region Medical Center /ID# 1128-1412
Jefferson City
North Carolina
Wake Forest Univ HS /ID# 1128-0975
Winston-salem
Nebraska
Nebraska Methodist Hospital /ID# 1128-0229
Omaha
New Jersey
New Jersey Center for Cancer Research /ID# 1128-0493
Brick
New Mexico
Duplicate_New Mexico Cancer Care Alliance /ID# 1128-0938
Albuquerque
San Juan Oncology Associates /ID# 1128-1020
Farmington
New York
Memorial Sloan Kettering Cancer Center-Koch Center /ID# 1128-0091
New York
Oregon
Oregon Health & Science University /ID# 1128-0251
Portland
Pennsylvania
Penn State Hershey Medical Ctr /ID# 1128-0220
Hershey
Abramson Cancer Center of the Univ. of Pennsylvania /ID# 1128-0402
Philadelphia
Tennessee
Vanderbilt Infectious Disease Clinic /ID# 1128-0024
Nashville
Texas
The University of Texas Medical Branch (UTMB) - Cancer Center - Galves /ID# 1128-0974
Galveston
Duplicate_Scott & White Mem Hosp & Clin /ID# 1128-0046
Temple
Virginia
Duplicate_Virginia Cancer Specialists - Fairfax Office /ID# 1128-0972
Fairfax
Washington
University of Washington /ID# 1128-1382
Seattle
Virginia Mason Medical Center /ID# 1128-0005
Seattle
Confluence Health /ID# 1128-0894
Wenatchee
Other Locations
Republic of Korea
Chonnam National University Hwasun Hospital /ID# 1128-0916
Jeonnam
Seoul National University Bundang Hospital /ID# 1128-0982
Seongnam
Asan Medical Center /ID# 1128-0963
Seoul
Korea University Guro Hospital /ID# 1128-0924
Seoul
Samsung Medical Center /ID# 1128-0925
Seoul
Seoul National University Hospital /ID# 1128-0926
Seoul
The Catholic University of Korea, Seoul St. Mary's Hospital /ID# 1128-0928
Seoul
Yonsei University Health System Severance Hospital /ID# 1128-0927
Seoul
Spain
Instituto Catalan de Oncologia (ICO) Badalona /ID# 1128-0984
Badalona
Hospital Clinic de Barcelona /ID# 1128-0533
Barcelona
Hospital Universitario Vall d'Hebron /ID# 1128-0534
Barcelona
Hospital Universitario 12 de Octubre /ID# 1128-0864
Madrid
Hospital Universitario La Paz /ID# 1128-0921
Madrid
Hospital Universitario Ramon y Cajal /ID# 1128-0874
Madrid
Hospital Unversitario Marques de Valdecilla /ID# 1128-0973
Santander
Hospital Universitario Virgen del Rocio /ID# 1128-0863
Sevilla
United Kingdom
Duplicate_Beatson west of scotland cancer center /ID# 1128-0652
Glasgow
Sarah Cannon Research Institute /ID# 1128-1079
London
The Royal Marsden NHS Foundation Trust /ID# 1128-0543
London
The Christie Hospital /ID# 1128-0030
Manchester
Duplicate_Oxford University Hospitals NHS Trust /ID# 1128-0814
Oxford
Time Frame
Start Date: 2015-12-01
Completion Date: 2021-08-20
Participants
Target number of participants: 263
Treatments
Experimental: Cohort 1: Renal Cell Carcinoma (RCC)
Phase 1b: Participants receive ibrutinib at various dose levels in combination with a fixed dose of everolimus to determine the recommended phase 2 dose (RP2D) of ibrutinib. (The RP2D was determined for each cohort separately.)~Phase 2: Participants receive ibrutinib at the RP2D determined in phase 1b in combination with everolimus.
Experimental: Cohort 2: Urothelial Carcinoma (UC)
Phase 1b: Participants receive ibrutinib at various dose levels in combination with a fixed dose of paclitaxel to determine the RP2D of ibrutinib. (The RP2D was determined for each cohort separately.)~Phase 2: Participants receive ibrutinib at the RP2D determined in Phase 1b in combination with paclitaxel.
Experimental: Cohort 3: Gastric Adenocarcinoma (GA or GC)
Phase 1b: Participants receive ibrutinib at various dose levels in combination with a fixed dose of docetaxel to determine the RP2D of ibrutinib. (The RP2D was determined for each cohort separately.)~Phase 2: Participants receive docetaxel at the RP2D determined in Phase 1b in combination with docetaxel.
Experimental: Cohort 4: Colorectal Adenocarcinoma (CRC)
Phase 1b: Participants receive ibrutinib at various dose levels in combination with a fixed dose of cetuximab to determine RP2D of ibrutinib. (The RP2D was determined for each cohort separately.)~Phase 2: Participants receive ibrutinib at the RP2D determined in Phase 1b in combination with cetuximab.
Experimental: Cohort 5: Urothelial Carcinoma (UC) Ibrutinib
Phase 1b: Participants receive ibrutinib at various dose levels to determine the RP2D of ibrutinib.(The RP2D was determined for each cohort separately.)~Phase 2: Participants receive ibrutinib at the RP2D determined in Phase 1b.
Experimental: Cohort 6: Urothelial Carcinoma (UC) With Pembrolizumab
Phase 1b: Participants receive ibrutinib at various dose levels in combination with a fixed dose of pembrolizumab to determine the RP2D of ibrutinib. (The RP2D was determined for each cohort separately.)~Phase 2: Participants receive ibrutinib at the RP2D determined in Phase 1b in combination with pembrolizumab.
Related Therapeutic Areas
Sponsors
Leads: Pharmacyclics LLC.

This content was sourced from clinicaltrials.gov

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